Trial intelligence / Profile preview

BAY 3401016 Phase 2a study in adults with Alport syndrome

2024-516471-33-00Phase 2Authorised

Sponsor
Bayer
Start
Jan 2026
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Countries
15
01

Overview

Phase 2, randomised, double-blind trial in Alport syndrome comparing BAY 3401016 with Placebo (2 arms). Primary endpoint: Mean UACR ratio to baseline averaged over 16, 20 and 24 weeks of treatment. Planned start Jan 2026; status: authorised.

02

Drugs

BAY 3401016
03

Conditions

Alport syndrome

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